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OpenTrials
Completed

NCT Number: NCT02355860

Female Sexual Function and Socioeconomic Status

In an urban gynecology practice serving patients with publicly and privately funded insurance, female sexual dysfunction was associated with low income, depression, urinary incontinence, and sexual inactivity.

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Observational

About this study

Introduction: Female sexual dysfunction is common, and the effect of socioeconomic status in an urban population is unknown. The objective is to determine socioeconomic and clinical factors associated with female sexual dysfunction for patients with publicly and privately funded health insurance in an urban outpatient gynecology clinic.

Methods: We performed an observational, IRB approved, cross-sectional study of 238 sexually-active, non-pregnant women reporting to two urban gynecology clinics, representing patients with publicly funded (n=70) or privately funded health insurance (n=168). The participants completed validated questionnaires measuring sexual function (Female Sexual Function Index or FSFI), depression (Center for Epidemiologic Studies Depression Scale), urinary incontinence (Questionnaire for Urinary Incontinence Diagnosis), and demographic variables. Data was analyzed with non-parametric t-tests, chi-squared tests, and linear regression models.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • women age 18 or older, presenting for an annual routine gynecology appointment, and were sexually active in the past six months

Exclusion criteria

  • pregnant women, women who were less than six weeks post-partum, women reporting for a gynecologic problem visit, non-English speakers, incomplete survey questionnaires, or refusal to consent to participate in the study.

Treatment and study plan

Assessment

Behavioral

assessment

Primary outcomes

  1. FSF Index

    Time frame: Day 1

    Questionnaire

Secondary outcomes

  1. Health Information Assessment

    Time frame: Day 1

    Questionnaire

Sponsors and collaborators

Lead sponsor

Brett Worly, MD

Other

Registry information

Important dates

Study start
2010
Primary completion
2010
Study completion
2010
First posted
Feb 4, 2015
Registry last updated
Feb 4, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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